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Accumulation of the RNA polymerase subunit RpoB depends on RNA editing by OsPPR16 and affects chloroplast development during early leaf development in rice

https://doi.org/10.1111/nph.16769
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/j.1460-2075.1994.tb06784.xopenalex-snapshot
Introduction of a heterologous editing site into the tobacco plastid genome: the lack of RNA editing leads to a mutant phenotype.
inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb00640.xopenalex-snapshot
Deletion of rpoB reveals a second distinct transcription system in plastids of higher plants.
inferredcites →https://doi.org/10.1006/abio.1976.9999openalex-snapshot
A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/4735_2007_0232openalex-snapshot
Transcription and transcriptional regulation in plastids
inferredcites →https://doi.org/10.1007/bf00015612openalex-snapshot
The chloroplast genome
inferredcites →https://doi.org/10.1007/s00122-010-1453-zopenalex-snapshot
Two complementary recessive genes in duplicated segments control etiolation in rice
inferredcites →https://doi.org/10.1007/s00239-005-0254-5openalex-snapshot
Sequence of the Tomato Chloroplast DNA and Evolutionary Comparison of Solanaceous Plastid Genomes
inferredcites →https://doi.org/10.1007/s004380000295openalex-snapshot
Conservation of RNA editing between rice and maize plastids: are most editing events dispensable?
inferredcites →https://doi.org/10.1007/s11099-017-0761-9openalex-snapshot
RNA editing of plastid-encoded genes
inferredcites →https://doi.org/10.1007/s11103-017-0654-0openalex-snapshot
OsPPR6, a pentatricopeptide repeat protein involved in editing and splicing chloroplast RNA, is required for chloroplast biogenesis in rice
inferredcites →https://doi.org/10.1007/s12010-016-2029-4openalex-snapshot
Reliable Selection and Holistic Stability Evaluation of Reference Genes for Rice Under 22 Different Experimental Conditions
inferredcites →https://doi.org/10.1016/0092-8674(93)90459-4openalex-snapshot
Signal transduction mutants of arabidopsis uncouple nuclear CAB and RBCS gene expression from chloroplast development
inferredcites →https://doi.org/10.1016/j.bbabio.2015.02.003openalex-snapshot
Insights into chloroplast biogenesis and development
inferredcites →https://doi.org/10.1016/j.bbabio.2015.02.004openalex-snapshot
Chloroplast RNA polymerases: Role in chloroplast biogenesis
inferredcites →https://doi.org/10.1016/j.febslet.2007.07.075openalex-snapshot
A hypothesis on the identification of the editing enzyme in plant organelles
inferredcites →https://doi.org/10.1016/j.febslet.2014.03.010openalex-snapshot
Phosphatidylglycerol biosynthesis is required for the development of embryos and normal membrane structures of chloroplasts and mitochondria in Arabidopsis
inferredcites →https://doi.org/10.1016/j.jplph.2015.04.001openalex-snapshot
Retrograde signaling between plastid and nucleus: A review
inferredcites →https://doi.org/10.1016/j.molp.2015.04.007openalex-snapshot
A Robust CRISPR/Cas9 System for Convenient, High-Efficiency Multiplex Genome Editing in Monocot and Dicot Plants
inferredcites →https://doi.org/10.1016/j.molp.2016.08.009openalex-snapshot
The RNA Editing Factor WSP1 Is Essential for Chloroplast Development in Rice
inferredcites →https://doi.org/10.1016/j.plantsci.2018.12.019openalex-snapshot
GRA78 encoding a putative S-sulfocysteine synthase is involved in chloroplast development at the early seedling stage of rice
inferredcites →https://doi.org/10.1016/j.tplants.2016.07.005openalex-snapshot
The Unexpected Diversity of Plant Organelle RNA Editosomes
inferredcites →https://doi.org/10.1016/s0014-5793(03)00480-0openalex-snapshot
A pentatricopeptide repeat‐containing gene that promotes the processing of aberrant atp6 RNA of cytoplasmic male‐sterile rice
inferredcites →https://doi.org/10.1016/s0074-7696(08)62145-2openalex-snapshot
Organellar RNA Polymerases of Higher Plants
inferredcites →https://doi.org/10.1023/a:1006297731456openalex-snapshot
Enzymes of chlorophyll biosynthesis
inferredcites →https://doi.org/10.1023/a:1013892009589openalex-snapshot
The genomics of land plant chloroplasts: Gene content and alteration of genomic information by RNA editing
inferredcites →https://doi.org/10.1038/36285openalex-snapshot
Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
inferredcites →https://doi.org/10.1038/nbt.2623openalex-snapshot
High-frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells
inferredcites →https://doi.org/10.1038/s41477-019-0415-yopenalex-snapshot
Control of retrograde signalling by protein import and cytosolic folding stress
inferredcites →https://doi.org/10.1038/s42003-019-0328-3openalex-snapshot
Plant-type pentatricopeptide repeat proteins with a DYW domain drive C-to-U RNA editing in Escherichia coli
inferredcites →https://doi.org/10.1046/j.1365-313x.1994.6020271.xopenalex-snapshot
Efficient transformation of rice ( Oryza sativa L.) mediated by Agrobacterium and sequence analysis of the boundaries of the T‐DNA
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01349.xopenalex-snapshot
Comparative analysis of plastid transcription profiles of entire plastid chromosomes from tobacco attributed to wild‐type and PEP‐deficient transcription machineries
inferredcites →https://doi.org/10.1073/pnas.0808529106openalex-snapshot
Chloroplast ribonucleoprotein CP31A is required for editing and stability of specific chloroplast mRNAs
inferredcites →https://doi.org/10.1073/pnas.1121465109openalex-snapshot
RIP1, a member of an Arabidopsis protein family, interacts with the protein RARE1 and broadly affects RNA editing
inferredcites →https://doi.org/10.1073/pnas.1202452109openalex-snapshot
Multiple organellar RNA editing factor (MORF) family proteins are required for RNA editing in mitochondria and plastids of plants
inferredcites →https://doi.org/10.1073/pnas.98.4.2053openalex-snapshot
Arabidopsis genomes uncoupled 5 ( GUN5 ) mutant reveals the involvement of Mg-chelatase H subunit in plastid-to-nucleus signal transduction
inferredcites →https://doi.org/10.1074/jbc.m114.631630openalex-snapshot
A Conserved Glutamate Residue in the C-terminal Deaminase Domain of Pentatricopeptide Repeat Proteins Is Required for RNA Editing Activity
inferredcites →https://doi.org/10.1074/jbc.m608034200openalex-snapshot
A Pentatricopeptide Repeat Protein Is Required for RNA Processing of clpP Pre-mRNA in Moss Chloroplasts
inferredcites →https://doi.org/10.1093/emboj/16.13.4041openalex-snapshot
The two RNA polymerases encoded by the nuclear and the plastid compartments transcribe distinct groups of genes in tobacco plastids
inferredcites →https://doi.org/10.1093/jxb/ery108openalex-snapshot
A Rice Dual-localized Pentatricopeptide Repeat Protein is involved in Organellar RNA Editing together with OsMORFs
inferredcites →https://doi.org/10.1093/jxb/ery139openalex-snapshot
ECD1 functions as an RNA-editing trans-factor of rps14-149 in plastids and is required for early chloroplast development in seedlings
inferredcites →https://doi.org/10.1093/jxb/ery214openalex-snapshot
WSL5, a pentatricopeptide repeat protein, is essential for chloroplast biogenesis in rice under cold stress
inferredcites →https://doi.org/10.1093/molbev/msr121openalex-snapshot
MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods
inferredcites →https://doi.org/10.1093/mp/ssu044openalex-snapshot
CRISPR-P: A Web Tool for Synthetic Single-Guide RNA Design of CRISPR-System in Plants
inferredcites →https://doi.org/10.1093/mp/ssu054openalex-snapshot
A Novel Chloroplast-Localized Pentatricopeptide Repeat Protein Involved in Splicing Affects Chloroplast Development and Abiotic Stress Response in Rice
inferredcites →https://doi.org/10.1093/nar/gkm1111openalex-snapshot
Impaired function of the phage-type RNA polymerase RpoTp in transcription of chloroplast genes is compensated by a second phage-type RNA polymerase
inferredcites →https://doi.org/10.1093/nar/gku402openalex-snapshot
CRISPR/Cas9 systems have off-target activity with insertions or deletions between target DNA and guide RNA sequences
inferredcites →https://doi.org/10.1093/nar/gkw270openalex-snapshot
A PPR protein in the PLS subfamily stabilizes the 5′-end of processedrpl16mRNAs in maize chloroplasts
inferredcites →https://doi.org/10.1093/pcp/pci070openalex-snapshot
Visualization of Plastid Nucleoids In situ Using the PEND–GFP Fusion Protein
inferredcites →https://doi.org/10.1104/pp.106.080069openalex-snapshot
The SCABRA3 Nuclear Gene Encodes the Plastid RpoTp RNA Polymerase, Which Is Required for Chloroplast Biogenesis and Mesophyll Cell Proliferation in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.085043openalex-snapshot
Building Up of the Plastid Transcriptional Machinery during Germination and Early Plant Development
inferredcites →https://doi.org/10.1104/pp.107.095737openalex-snapshot
AWUSCHEL-LIKE HOMEOBOXGene Represses aYABBYGene Expression Required for Rice Leaf Development
inferredcites →https://doi.org/10.1104/pp.107.103846openalex-snapshot
Phage-Type RNA Polymerase RPOTmp Transcribes the rrn Operon from the PC Promoter at Early Developmental Stages in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.136812openalex-snapshot
LPA66 Is Required for EditingpsbFChloroplast Transcripts in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.111.188474openalex-snapshot
Nucleoid-Enriched Proteomes in Developing Plastids and Chloroplasts from Maize Leaves: A New Conceptual Framework for Nucleoid Functions
inferredcites →https://doi.org/10.1104/pp.112.195081openalex-snapshot
Disruption of a Rice Pentatricopeptide Repeat Protein Causes a Seedling-Specific Albino Phenotype and Its Utilization to Enhance Seed Purity in Hybrid Rice Production
inferredcites →https://doi.org/10.1104/pp.113.228726openalex-snapshot
A Major Role for the Plastid-Encoded RNA Polymerase Complex in the Expression of Plastid Transfer RNAs
inferredcites →https://doi.org/10.1104/pp.15.00354openalex-snapshot
The SLOW GROWTH3 Pentatricopeptide Repeat Protein Is Required for the Splicing of Mitochondrial NADH Dehydrogenase Subunit7 Intron 2 in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.15.01949openalex-snapshot
WHITE PANICLE1, a Val-tRNA Synthetase Regulating Chloroplast Ribosome Biogenesis in Rice, Is Essential for Early Chloroplast Development
inferredcites →https://doi.org/10.1104/pp.16.01625openalex-snapshot
A Rice PECTATE LYASE-LIKE Gene Is Required for Plant Growth and Leaf Senescence
inferredcites →https://doi.org/10.1104/pp.16.01840openalex-snapshot
The Pentatricopeptide Repeat Protein EMB2654 Is Essential for Trans-Splicing of a Chloroplast Small Ribosomal Subunit Transcript
inferredcites →https://doi.org/10.1104/pp.18.00009openalex-snapshot
Control of Retrograde Signaling by Rapid Turnover of GENOMES UNCOUPLED1
inferredcites →https://doi.org/10.1104/pp.18.01432openalex-snapshot
Highly Resolved Systems Biology to Dissect the Etioplast-to-Chloroplast Transition in Tobacco Leaves
inferredcites →https://doi.org/10.1104/pp.19.00070openalex-snapshot
Extrachloroplastic PP7L Functions in Chloroplast Development and Abiotic Stress Tolerance
inferredcites →https://doi.org/10.1104/pp.19.00421openalex-snapshot
Extensive Posttranscriptional Regulation of Nuclear Gene Expression by Plastid Retrograde Signals
inferredcites →https://doi.org/10.1104/pp.19.00922openalex-snapshot
Establishment of a Heterologous RNA Editing Event in Chloroplasts
inferredcites →https://doi.org/10.1105/tpc.105.033910openalex-snapshot
Arabidopsis SENESCENCE-ASSOCIATED GENE101 Stabilizes and Signals within an ENHANCED DISEASE SUSCEPTIBILITY1 Complex in Plant Innate Immunity
inferredcites →https://doi.org/10.1105/tpc.108.064667openalex-snapshot
Pentatricopeptide Repeat Proteins with the DYW Motif Have Distinct Molecular Functions in RNA Editing and RNA Cleavage in Arabidopsis Chloroplasts
inferredcites →https://doi.org/10.1105/tpc.111.089441openalex-snapshot
The Primary Transcriptome of Barley Chloroplasts: Numerous Noncoding RNAs and the Dominating Role of the Plastid-Encoded RNA Polymerase
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03529.xopenalex-snapshot
Suppression mechanism of mitochondrial ORF79 accumulation by Rf1 protein in BT‐type cytoplasmic male sterile rice
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03634.xopenalex-snapshot
CLB19, a pentatricopeptide repeat protein required for editing of rpoA and clpP chloroplast transcripts
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03766.xopenalex-snapshot
The Arabidopsis gene YS1 encoding a DYW protein is required for editing of rpoB transcripts and the rapid development of chloroplasts during early growth
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05091.xopenalex-snapshot
Rice MPR25 encodes a pentatricopeptide repeat protein and is essential for RNA editing of nad5 transcripts in mitochondria
inferredcites →https://doi.org/10.1111/j.1399-3054.1962.tb08052.xopenalex-snapshot
A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures
inferredcites →https://doi.org/10.1111/nph.13468openalex-snapshot
Functional analysis of the Arabidopsis thaliana CHLOROPLAST BIOGENESIS 19 pentatricopeptide repeat editing protein
inferredcites →https://doi.org/10.1111/nph.15448openalex-snapshot
The RNA editing factor DUA 1 is crucial to chloroplast development at low temperature in rice
inferredcites →https://doi.org/10.1111/nph.15814openalex-snapshot
Rice FLOURY ENDOSPERM 10 encodes a pentatricopeptide repeat protein that is essential for the trans‐splicing of mitochondrial nad1 intron 1 and endosperm development
inferredcites →https://doi.org/10.1111/plb.12978openalex-snapshot
Mutation of the rice TCM 12 gene encoding 2,3‐bisphosphoglycerate‐independent phosphoglycerate mutase affects chlorophyll synthesis, photosynthesis and chloroplast development at seedling stage at low temperatures
inferredcites →https://doi.org/10.1111/tpj.12001openalex-snapshot
FtsHi1/ARC1 is an essential gene in Arabidopsis that links chloroplast biogenesis and division
inferredcites →https://doi.org/10.1111/tpj.12756openalex-snapshot
AEF 1/ MPR 25 is implicated in RNA editing of plastid atpF and mitochondrial nad5 , and also promotes atpF splicing in Arabidopsis and rice
inferredcites →https://doi.org/10.1111/tpj.13093openalex-snapshot
The PPR ‐ SMR protein PPR 53 enhances the stability and translation of specific chloroplast RNA s in maize
inferredcites →https://doi.org/10.1111/tpj.13126openalex-snapshot
SOT 1, a pentatricopeptide repeat protein with a small MutS‐related domain, is required for correct processing of plastid 23S–4.5S rRNA precursors in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.13185openalex-snapshot
The Restorer‐of‐fertility‐like 2 pentatricopeptide repeat protein and RN ase P are required for the processing of mitochondrial orf291 RNA in Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.13884openalex-snapshot
An evolutionarily conserved P‐subfamily pentatricopeptide repeat protein is required to splice the plastid ndhA transcript in the moss Physcomitrella patens and Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.14030openalex-snapshot
The pentatricopeptide repeat protein EMPTY PERICARP 8 is required for the splicing of three mitochondrial introns and seed development in maize
inferredcites →https://doi.org/10.1111/tpj.14384openalex-snapshot
Stable native RIP 9 complexes associate with C‐to‐U RNA editing activity, PPR s, RIP s, OZ 1, ORRM 1 and ISE 2
inferredcites →https://doi.org/10.1111/tpj.14578openalex-snapshot
Plant organellar RNA editing: what 30 years of research has revealed
inferredcites →https://doi.org/10.1126/science.1079978openalex-snapshot
GUN4, a Regulator of Chlorophyll Synthesis and Intracellular Signaling
inferredcites →https://doi.org/10.1126/science.1219021openalex-snapshot
The Protein-Folding Problem, 50 Years On
inferredcites →https://doi.org/10.1126/science.277.5327.809openalex-snapshot
Mitochondrial and Chloroplast Phage-Type RNA Polymerases in Arabidopsis
inferredcites →https://doi.org/10.1126/science.aaw7166openalex-snapshot
Cytosine, but not adenine, base editors induce genome-wide off-target mutations in rice
inferredcites →https://doi.org/10.1128/mcb.00563-08openalex-snapshot
The Pentatricopeptide Repeat Protein PPR5 Stabilizes a Specific tRNA Precursor in Maize Chloroplasts
inferredcites →https://doi.org/10.1146/annurev-arplant-050213-040159openalex-snapshot
Pentatricopeptide Repeat Proteins in Plants
inferredcites →https://doi.org/10.1186/1471-2229-7-37openalex-snapshot
Mutations in a plastid-localized elongation factor G alter early stages of plastid development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1186/1746-4811-7-30openalex-snapshot
A highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes
inferredcites →https://doi.org/10.1186/s12284-015-0050-9openalex-snapshot
The rice ALS3 encoding a novel pentatricopeptide repeat protein is required for chloroplast development and seedling growth
inferredcites →https://doi.org/10.1186/s12284-018-0237-yopenalex-snapshot
Overexpression of OsbHLH107, a member of the basic helix-loop-helix transcription factor family, enhances grain size in rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1186/s12864-018-5088-9openalex-snapshot
Genome-wide analysis of the rice PPR gene family and their expression profiles under different stress treatments
inferredcites →https://doi.org/10.1186/s13059-016-1004-2openalex-snapshot
Chloroplast genomes: diversity, evolution, and applications in genetic engineering
inferredcites →https://doi.org/10.1261/rna.1533909openalex-snapshot
A comparative genomics approach identifies a PPR-DYW protein that is essential for C-to-U editing of the Arabidopsis chloroplast accD transcript
inferredcites →https://doi.org/10.1261/rna.823508openalex-snapshot
Faithful editing of a tomato-specific mRNA editing site in transgenic tobacco chloroplasts
inferredcites →https://doi.org/10.1371/journal.pgen.1002910openalex-snapshot
A Combinatorial Amino Acid Code for RNA Recognition by Pentatricopeptide Repeat Proteins
inferredcites →https://doi.org/10.3389/fpls.2014.00667openalex-snapshot
AtSIG6 and other members of the sigma gene family jointly but differentially determine plastid target gene expression in Arabidopsis thaliana
inferredcites →https://doi.org/10.3389/fpls.2017.01116openalex-snapshot
WHITE STRIPE LEAF4 Encodes a Novel P-Type PPR Protein Required for Chloroplast Biogenesis during Early Leaf Development
inferredcites →https://doi.org/10.3389/fpls.2018.00841openalex-snapshot
Editing of Chloroplast rps14 by PPR Editing Factor EMB2261 Is Essential for Arabidopsis Development
inferredcites →https://doi.org/10.3390/genes8010005openalex-snapshot
RNA Editing and Its Molecular Mechanism in Plant Organelles
inferredcites →https://doi.org/10.5511/plantbiotechnology.12.1217aopenalex-snapshot
A pentatricopeptide repeat gene of rice is required for splicing of chloroplast transcripts and RNA editing of ndhA
inferredcites →https://doi.org/10.7554/elife.08504openalex-snapshot
Structure of a bacterial RNA polymerase holoenzyme open promoter complex

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4780645openalex-extracted
A Novel Pls-Dyw Type Ppr Protein Osasl Is Essential for Chloroplast Development in Rice
inferred← citeshttps://doi.org/10.1007/s00425-022-03926-yopenalex-snapshot
Same modification, different location: the mythical role of N6-adenine methylation in plant genomes
inferred← citeshttps://doi.org/10.1007/s00425-025-04634-zopenalex-snapshot
Dek570-1, a PPR-DYW protein, is required for maize seed and plant development via modulation of C-to-U RNA editing in mitochondria and chloroplasts
inferred← citeshttps://doi.org/10.1007/s10681-024-03379-2openalex-snapshot
TAG encodes an adenine nucleotide transport protein that regulates leaf color in rice
inferred← citeshttps://doi.org/10.1007/s11032-024-01468-7openalex-snapshot
OsPGL3A encodes a DYW-type pentatricopeptide repeat protein involved in chloroplast RNA processing and regulated chloroplast development
inferred← citeshttps://doi.org/10.1007/s11103-025-01561-1openalex-snapshot
Barley young leaf chlorina, a putative pentatricopeptide repeat gene, is essential for chloroplast development in young leaves
inferred← citeshttps://doi.org/10.1007/s12374-026-09515-wopenalex-snapshot
Young Seedling Stripe3 Encodes a Chloroplast-localized Multiple Organellar RNA Editing Factor Essential for Chloroplast RNA Editing and Splicing in Rice
inferred← citeshttps://doi.org/10.1007/s40626-024-00328-1openalex-snapshot
Gene expression and physiological roles of post-transcriptional editing in plant organellar systems
inferred← citeshttps://doi.org/10.1016/j.cj.2023.04.009openalex-snapshot
OsTHA8 encodes a pentatricopeptide repeat protein required for RNA editing and splicing during rice chloroplast development
inferred← citeshttps://doi.org/10.1016/j.cj.2025.06.015openalex-snapshot
The pentatricopeptide repeat protein AL5 modulates early chloroplast development in rice
inferred← citeshttps://doi.org/10.1016/j.cpb.2025.100540openalex-snapshot
Gene editing tools promote the development of chloroplast gene engineering
inferred← citeshttps://doi.org/10.1016/j.gene.2022.146898openalex-snapshot
Genome-wide identification of RNA editing sites in chloroplast transcripts and multiple organellar RNA editing factors in tea plant (Camellia sinensis L.): Insights into the albinism mechanism of tea leaves
inferred← citeshttps://doi.org/10.1016/j.jia.2022.08.005openalex-snapshot
OsDXR interacts with OsMORF1 to regulate chloroplast development and the RNA editing of chloroplast genes in rice
inferred← citeshttps://doi.org/10.1016/j.jia.2022.08.026openalex-snapshot
OsPPR9 encodes a DYW-type PPR protein that affects editing efficiency of multiple RNA editing sites and is essential for chloroplast development
inferred← citeshttps://doi.org/10.1016/j.jia.2026.03.042openalex-snapshot
Mutation in CmPPR confers a yellow-leaf phenotype and chloroplast defects in melon (Cucumis melo L.)
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.110908openalex-snapshot
PPR protein Early Chloroplast Development 2 is essential for chloroplast development at the early stage of Arabidopsis development
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112134openalex-snapshot
A novel PLS-DYW type PPR protein OsASL is essential for chloroplast development in rice
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112263openalex-snapshot
Emerging roles of the C-to-U RNA editing in plant stress responses
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112478openalex-snapshot
GhCTEF2 encodes a PLS-type PPR protein required for chloroplast development and plastid RNA editing in cotton
inferred← citeshttps://doi.org/10.1016/j.rsci.2023.11.011openalex-snapshot
Analysis of RNA Recognition and Binding Characteristics of OsCPPR1 Protein in Rice
inferred← citeshttps://doi.org/10.1016/j.xplc.2024.100858openalex-snapshot
GhCTSF1, a short PPR protein with a conserved role in chloroplast development and photosynthesis, participates in intron splicing of rpoC1 and ycf3-2 transcripts in cotton
inferred← citeshttps://doi.org/10.1016/j.xplc.2024.101073openalex-snapshot
The chloroplast pentatricopeptide repeat protein RCN22 regulates tiller number in rice by affecting sugar levels via the TB1–RCN22–RbcL module
inferred← citeshttps://doi.org/10.1038/s41598-026-52125-2openalex-snapshot
Anatomy and the chloroplast genome of Bischofia plants reveal important phylogenetic relationship and the genetic diversity in phyllanthaceae
inferred← citeshttps://doi.org/10.1073/pnas.2208759119openalex-snapshot
Fujian cytoplasmic male sterility and the fertility restorer gene OsRf19 provide a promising breeding system for hybrid rice
inferred← citeshttps://doi.org/10.1093/hr/uhae006openalex-snapshot
Chloroplast C-to-U editing, regulated by a PPR protein BoYgl-2, is important for chlorophyll biosynthesis in cabbage
inferred← citeshttps://doi.org/10.1093/hr/uhaf194openalex-snapshot
SlPPR138-mediated RNA editing of rpoC1 is essential for chloroplast development in tomato
inferred← citeshttps://doi.org/10.1093/jxb/erab185openalex-snapshot
ZmPPR26, a DYW-type pentatricopeptide repeat protein, is required for C-to-U RNA editing at atpA-1148 in maize chloroplasts
inferred← citeshttps://doi.org/10.1093/jxb/erab502openalex-snapshot
Dissecting the genetic control of natural variation in sorghum photosynthetic response to drought stress
inferred← citeshttps://doi.org/10.1093/plphys/kiag205openalex-snapshot
Interacting with GUN1 and MORF2, SL1 modulates plastid RNA editing during norflurazon-induced retrograde signaling
inferred← citeshttps://doi.org/10.1101/2024.11.08.622588openalex-snapshot
OsMORF protein selectively promotes the dual-localized RNA editing factor OsPGL1 binding to its target RNA
inferred← citeshttps://doi.org/10.1111/nph.70744openalex-snapshot
A temperature‐sensitive complex formed by OsDYW2 is required for chloroplast RNA editing and splicing under high temperature in rice
inferred← citeshttps://doi.org/10.1111/ppl.14064openalex-snapshot
Integrative transcriptome and whole‐genome bisulfite sequencing analyses of a temperature‐sensitive albino tea plant cultivar
inferred← citeshttps://doi.org/10.1111/tpj.70246openalex-snapshot
OsPPR8 , a pentatricopeptide repeat protein, regulates splicing of mitochondrial nad2 intron 3 to affect grain quality and high‐temperature tolerance in rice
inferred← citeshttps://doi.org/10.1111/tpj.70526openalex-snapshot
A six‐repeat PPR protein WPR directly binds target RNAs and coordinates chloroplast RNA processing via dual recruitment of MORF1 , MORF8b , and CAF2 proteins in rice
inferred← citeshttps://doi.org/10.1166/jbmb.2022.2167openalex-snapshot
Cytological Observation and Candidate Gene Identification of a Female Semi-Sterile Rice Mutant
inferred← citeshttps://doi.org/10.1186/s12284-021-00489-6openalex-snapshot
Plastid caseinolytic protease OsClpR1 regulates chloroplast development and chloroplast RNA editing in rice
inferred← citeshttps://doi.org/10.1186/s12870-022-03742-2openalex-snapshot
Chloroplastic pentatricopeptide repeat proteins (PPR) in albino plantlets of Agave angustifolia Haw. reveal unexpected behavior
inferred← citeshttps://doi.org/10.1186/s12870-022-03819-yopenalex-snapshot
A chloroplast-localized pentatricopeptide repeat protein involved in RNA editing and splicing and its effects on chloroplast development in rice
inferred← citeshttps://doi.org/10.1186/s12870-025-06657-wopenalex-snapshot
Weighted gene co-expression network analysis − based selection of hub genes related to phenolic and volatile compounds and seed coat color in sorghum
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3364853/v1openalex-snapshot
A chimeric mitochondrial gene FA323 confers male sterility in Fujian cytoplasmic male sterile rice
inferred← citeshttps://doi.org/10.3389/fgene.2021.765580openalex-snapshot
Research Progress of PPR Proteins in RNA Editing, Stress Response, Plant Growth and Development
inferred← citeshttps://doi.org/10.3389/fgene.2022.869465openalex-snapshot
An Insight Into Pentatricopeptide-Mediated Chloroplast Necrosis via microRNA395a During Rhizoctonia solani Infection
inferred← citeshttps://doi.org/10.3389/fpls.2021.627501openalex-snapshot
Functioning of PPR Proteins in Organelle RNA Metabolism and Chloroplast Biogenesis
inferred← citeshttps://doi.org/10.3389/fpls.2021.700975openalex-snapshot
A Novel Chloroplast Protein RNA Processing 8 Is Required for the Expression of Chloroplast Genes and Chloroplast Development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2022.918673openalex-snapshot
WATER-SOAKED SPOT1 Controls Chloroplast Development and Leaf Senescence via Regulating Reactive Oxygen Species Homeostasis in Rice
inferred← citeshttps://doi.org/10.3389/fpls.2024.1416742openalex-snapshot
PPR proteins in plants: roles, mechanisms, and prospects for rice research
inferred← citeshttps://doi.org/10.3389/fpls.2026.1767760openalex-snapshot
Genome-wide identification and dynamic transcriptome profiling of the DYW-type PPR family across greening of chlorotic leaves in pear (Pyrus pyrifolia)
inferred← citeshttps://doi.org/10.3390/agriculture16192045openalex-snapshot
ZmWGSL2 Is a Candidate Chloroplast-Localized PPR Gene Associated with Chloroplast Development and Leaf-Colour Formation in Maize
inferred← citeshttps://doi.org/10.3390/cimb44110379openalex-snapshot
RNA Editing in Chloroplast: Advancements and Opportunities
inferred← citeshttps://doi.org/10.3390/ijms222413648openalex-snapshot
Plastid Deficient 1 Is Essential for the Accumulation of Plastid-Encoded RNA Polymerase Core Subunit β and Chloroplast Development in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms241914457openalex-snapshot
Integrated Cytological, Physiological, and Transcriptome Analyses Provide Insight into the Albino Phenotype of Chinese Plum (Prunus salicina)
inferred← citeshttps://doi.org/10.3390/plants14111634openalex-snapshot
Chloroplast-Localized Protein, OsAL7, with Two Elongation Factor Thermostable Domains Is Essential for Normal Chloroplast Development and Seedling Longevity in Oryza sativa
inferred← citeshttps://doi.org/10.3390/plants15020284openalex-snapshot
CDE6 Regulates Chloroplast Ultrastructure and Affects the Sensitivity of Rice to High Temperature
inferred← citeshttps://doi.org/10.3390/plants15131936openalex-snapshot
From Ethnobotany to Pharmacognosy: A Review of Firmiana colorata
inferred← citeshttps://doi.org/10.48130/seedbio-0024-0018openalex-snapshot
Exploiting male sterility toward the development of hybrid rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.14633966openalex-snapshot
Additional file 1 of Plastid caseinolytic protease OsClpR1 regulates chloroplast development and chloroplast RNA editing in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.20336909openalex-snapshot
Additional file 1 of Chloroplastic pentatricopeptide repeat proteins (PPR) in albino plantlets of Agave angustifolia Haw. reveal unexpected behavior
inferred← citeshttps://doi.org/10.6084/m9.figshare.21087501openalex-snapshot
Additional file 1 of A chloroplast-localized pentatricopeptide repeat protein involved in RNA editing and splicing and its effects on chloroplast development in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.21087504openalex-snapshot
Additional file 2 of A chloroplast-localized pentatricopeptide repeat protein involved in RNA editing and splicing and its effects on chloroplast development in rice
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